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Structural Alterations in the Translational Attenuator of Constitutively Expressed ErmC Genes

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Specialty Pharmacology
Date 1999 Jul 2
PMID 10390222
Citations 20
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Abstract

Sequence deletions of 16, 59, and 111 bp as well as a tandem duplication of 272 bp with respect to the corresponding sequence of pT48 were identified in the regulatory regions of constitutively expressed ermC genes. Constitutive ermC gene expression as a consequence of these structural alterations is based on either the prevention of the formation of mRNA secondary structures in the translational attenuator or the preferential formation of those mRNA secondary structures which do not interfere with the translation of the ermC transcripts. A model for the development of sequence deletions in the ermC translational attenuator by homologous recombination is presented and experimentally tested by in vitro selection of constitutively expressed mutants in staphylococcal strains deficient and proficient in homologous recombination.

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References
1.
Monod M, Denoya C, Dubnau D . Sequence and properties of pIM13, a macrolide-lincosamide-streptogramin B resistance plasmid from Bacillus subtilis. J Bacteriol. 1986; 167(1):138-47. PMC: 212852. DOI: 10.1128/jb.167.1.138-147.1986. View

2.
Weisblum B . Inducible resistance to macrolides, lincosamides and streptogramin type B antibiotics: the resistance phenotype, its biological diversity, and structural elements that regulate expression--a review. J Antimicrob Chemother. 1985; 16 Suppl A:63-90. DOI: 10.1093/jac/16.suppl_a.63. View

3.
Allen N . Macrolide resistance in Staphylococcus aureus: inducers of macrolide resistance. Antimicrob Agents Chemother. 1977; 11(4):669-74. PMC: 352047. DOI: 10.1128/AAC.11.4.669. View

4.
Weisblum B . Insights into erythromycin action from studies of its activity as inducer of resistance. Antimicrob Agents Chemother. 1995; 39(4):797-805. PMC: 162632. DOI: 10.1128/AAC.39.4.797. View

5.
Lodder G, Werckenthin C, Schwarz S, Dyke K . Molecular analysis of naturally occuring ermC-encoding plasmids in staphylococci isolated from animals with and without previous contact with macrolide/lincosamide antibiotics. FEMS Immunol Med Microbiol. 1997; 18(1):7-15. DOI: 10.1111/j.1574-695X.1997.tb01022.x. View